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1 the left posterior superior temporal cortex (Wernicke's area).
2 rior temporal regions bilaterally (including Wernicke's area).
3 demonstrated SSC's superiority at localizing Wernicke's area.
4 risk allele, p=7.64x10(-5)), which contains Wernicke's area.
5 ic error production to lesions in and around Wernicke's area.
6 erior and middle temporal gyri, in classical Wernicke's area.
7 e temporal and angular gyri corresponding to Wernicke's area.
8 n the superior temporal gyrus, the so-called Wernicke's area.
9 essive right-sided activation of Broca's and Wernicke's areas.
10 other motor regions, and between Broca's and Wernicke's areas.
11 emporal/fusiform gyrus, Broca's area, and/or Wernicke's area accounted for most acute improvement aft
12 he temporal-lobe language-sensitive regions (Wernicke's area) also show effectively little or no sepa
14 ds); (2) the VWFA has preferential RSFC with Wernicke's area and other core regions of the language s
15 and verbal fluency (FAS), in localizing the Wernicke's area and studied the association between geno
16 the left posterior superior temporal gyrus (Wernicke's area) and motor production processes occurred
17 -correlated activity with auditory (only for Wernicke's area) and visual cortices that suggests integ
18 ociative bundle connecting Broca's area with Wernicke's area, and other language regions of the tempo
19 (the left laterosuperior temporal cortex, or Wernicke's area, and the left inferior frontal gyrus, or
20 four regions of interest (ROIs): Broca's and Wernicke's areas, and their anatomic homologues in the r
21 n various Brodmann's areas--BA 22 (including Wernicke's area), BA 44 (part of Broca's area), BA 45 (p
22 l links with posterior language areas (e.g., Wernicke's area), because it is presumed to be involved
23 y encompassing temporoparietal components of Wernicke's area, Broca's area, and dorsal premotor corte
24 add further evidence for the crucial role of Wernicke's area (Brodmann's area 22) in word comprehensi
25 demonstrated foci not only within classical Wernicke's area but also within the middle and inferior
26 nd not only in language regions (Broca's and Wernicke's areas), but also specific regions in bilatera
27 largely agree with the classical notion that Wernicke's area, defined here as middle superior tempora
28 sical arcuate pathway connecting Broca's and Wernicke's areas directly, we show a previously undescri
29 r, a memory-specific left-sided dominance in Wernicke's area for speech perception has been demonstra
30 guage processing regions such as Broca's and Wernicke's areas for the word problems and the horizonta
32 the functional and anatomical boundaries of 'Wernicke's area' have become so broad as to be meaningle
35 Our results highlight the important role of Wernicke's area in forming vivid musical imagery through
36 lization (e.g. Broca's area in the left, and Wernicke's area in the right hemisphere) have been repor
37 humans, Broca's area in the frontal lobe and Wernicke's area in the temporal lobe are crucially invol
42 arietal areas, traditionally included within Wernicke's area, leave single word comprehension intact
44 On one hand, fronto-temporal projections to Wernicke's area may not be unique to the arcuate fascicu
46 with the magnitude of delay in perfusion of Wernicke's area on magnetic resonance perfusion-weighted
48 he strength of the RSFC between the VWFA and Wernicke's area predicts performance on a semantic class
50 bidirectional connection between Broca's and Wernicke's areas probably through the arcuate fasciculus
51 cal network, but independently of awareness, Wernicke's area processes predictive events in time and
52 oca's area) and posterior superior temporal (Wernicke's area) regions, in addition to other language
53 in time-to-peak concentration of contrast in Wernicke's area, relative to the homologous region on th
55 ith a different functional specificity; e.g. Wernicke's area responded specifically to speech sounds
56 Language areas of the brain (Broca's and Wernicke's area) responded as the premises and the concl
57 internal capsule (RR, 2.2; 95% CI, 1.1-4.4), Wernicke's area (RR, 2.0; 95% CI, 1.1-3.8), or basal gan
58 because of its functional connectivity with Wernicke's area.SIGNIFICANCE STATEMENT The visual word f
59 n the thalamus and Broca's area extending to Wernicke's area, supporting the hypothesized (negative)
60 ge functional connectivity (except posterior Wernicke's area that exhibited predominant long-range co
61 tivity was left lateralized (except anterior Wernicke's area that exhibited rightward lateralization)
62 lative underactivation in posterior regions (Wernicke's area, the angular gyrus, and striate cortex)
63 Transmodal areas in the midtemporal cortex, Wernicke's area, the hippocampal-entorhinal complex and
64 arcuate fasciculus, which links Broca's and Wernicke's areas, the core neocortical language regions
65 vealed a posterior superior temporal region (Wernicke's area, traditionally considered a language-spe
66 area versus its right-hemisphere homolog and Wernicke's area versus its right-hemisphere homolog.
69 the presence of hypoperfusion or infarct in Wernicke's area, we tested the hypothesis that the sever
70 ng activations at the anterolateral belt and Wernicke's area, where the responses were correlated wit